Localized surface annealing of components for substrate processing chambers

Information

  • Patent Grant
  • 8617672
  • Patent Number
    8,617,672
  • Date Filed
    Wednesday, July 13, 2005
    19 years ago
  • Date Issued
    Tuesday, December 31, 2013
    10 years ago
Abstract
A substrate processing chamber component has a structural body with localized surface regions having annealed microcracks. The annealed microcracks reduce crack propagation and increase fracture resistance. In one method of manufacture, the structural body of the component is formed, and a laser beam is directed onto localized surface regions of the body for a sufficient time to anneal the surface microcracks.
Description
BACKGROUND

Embodiments of the present invention relate to components for substrate processing chambers.


A substrate processing chamber is used to process a substrate such as for example, a semiconductor wafer or display, in an energized process gas. The processing chamber typically comprises an enclosure wall that encloses a process zone into which a gas is introduced and energized. The chamber may be used to deposit material on the substrate by chemical or physical vapor deposition, etch material from a substrate, implant material on a substrate, or convert substrate layers such as by oxidizing layers or forming nitrides. The chamber typically includes a number of internal chamber components such as for example, a substrate support, gas distributor, gas energizer, and different types of liners and shields. For example, the liners and shields can be cylindrical members surrounding the substrate to serve as focus rings to direct and contain plasma about the substrate, deposition rings that prevent deposition on underlying components or portions of the substrate, substrate shields, and chamber wall liners.


Ceramic materials are often used to form the internal chamber components, especially those components that are exposed to the energized gas or plasma, and consequently, are subject to high temperatures and erosion. Ceramic materials such as alumina and silica are crystalline whereas silica glasses have no long range order. Ceramics typically exhibit good resistance to erosion by the energized gases, and consequently, do not have to be replaced as often as metal alloys. Ceramic components also reduce the generation of particles in the chamber that result from the erosion of components. Ceramic components can also withstand high temperatures without thermal degradation. Quartz components are particularly useful for plasmas that would corrode other materials, such as plasmas containing fluorine species.


However, ceramic materials are subject to brittle failure modes and often crack or chip in use in the chamber or during handling in the replacement or cleaning of the component. Amorphous and microcrystalline materials are particularly susceptible to brittle failure through crack propagation. In amorphous materials, such as glass, surface microcracks propagate on an atomic level because glass has short-range order without any long-range order. Microcrystalline materials, such as quartz, have grains with surface that can have intragranular microcracks that are through single grains, intergranular microcracks that extend around grains and along grain boundaries, as well as transgranular microcracks that cut across adjacent grains. Of these, the intergranular microcracks that extend around the microcrystalline grains of the quartz are generally the most culpable for crack propagation and often lead to chipping and cracking of the component.


Thus, it is desirable to have a ceramic component made from microcrystalline or amorphous ceramics that exhibits reduced chipping and cracking. It is further desirable to fabricate such ceramic components with lower failure rates during use. It is also desirable for the ceramic components to be able to withstand the energized gas environment in the chamber without excessive erosion or thermal degradation.


SUMMARY

A substrate processing chamber component has a structural body with localized surface regions having annealed microcracks. The annealed microcracks reduce crack propagation and increase fracture resistance. The structural body of the component is formed, and a laser beam is directed onto localized surface regions of the component for a sufficient time to anneal the surface microcracks. This will result in strengthening of the material and increased life of the component. Suitable lasers include CO2 and argon lasers. The structural body can be made of crystalline ceramic, glass, or glass-ceramic materials, for example, the body can be a ring made from quartz.





DRAWINGS

These features, aspects, and advantages of the present invention will become better understood with regard to the following description, appended claims, and accompanying drawings, which illustrate examples of the invention. However, it is to be understood that each of the features can be used in the invention in general, not merely in the context of the particular drawings, and the invention includes any combination of these features, where:



FIG. 1A is a cross-sectional schematic view of a chamber component made from glass showing microcracks in the surface of the glass;



FIG. 1B is a cross-sectional schematic view of the chamber component of FIG. 1A after localized laser treatment to anneal the surface microcracks;



FIG. 1C is a cross-sectional schematic view of a chamber component made from quartz showing microcracks along the grains and grain boundary regions of the quartz;



FIG. 1D is a cross-sectional schematic view of the chamber component of FIG. 1C after localized laser treatment to anneal the surface microcracks;



FIG. 2 is a perspective view of a quartz ring having a laser annealed surface;



FIGS. 3A and 3B are optical microscopy images of a quartz surface with surface microcracks before and after laser treatment, respectively;



FIG. 4 is a schematic view of a laser annealing apparatus suitable for localized surface annealing of the chamber component;



FIG. 5 is a sectional schematic view of a substrate processing chamber that uses the ring of FIG. 2; and



FIG. 6 is a schematic partial sectional side view of support assembly that uses the ring of FIG. 2 in the chamber of FIG. 5.





DESCRIPTION

A substrate processing chamber component 20 comprises a structural body 24 with localized surface regions 26 having microcracks 28, as shown in FIGS. 1A to 1D. The chamber component 20 can be made from a ceramic, glass or glass ceramic material, such as for example, quartz, silica glass, aluminum oxide, titanium oxide, silicon nitride, zirconium oxide, and other such materials. The surface microcracks 28 are caused by fine dust or other abrasive materials that strike and abrade the component surface 26 during or after fabrication of the component. FIG. 1A shows a component 20 made from glass, which is amorphous and has short range atomic order but no long range atomic order. For example, silica glass has short range order within individual silica tetrahedrons with fixed silicon and oxygen bond angles, but the silica tetrahedral may be interconnected with random bond angles. In glass, the microcracks are very fine and terminate with atomic bonds. Microcrystalline ceramic materials, as shown in FIG. 1C, are polycrystalline with fine grains 29 having micron sized dimensions. In microcrystalline materials, the microcracks 28 typically extend around the fine grains 29 and or along grain boundaries 31, but they can also cut across single or adjacent grains 29. The surface microcracks 28 on the components 20 serve as stress concentrators that cause applied forces to concentrate on the tips of the microcracks 20. Because the dimensions of the microcracks 28 are very small, on the level of atomic bonds between atoms of the component material in glass materials, and on the level of micron sized grains in microcrystalline materials, the applied stress is magnified tremendously at the crack tip. This results in rapid catastrophic failure modes in which a portion of the component 20 can easily crack or chip away with even a small applied force or impact.


In one exemplary embodiment, the component 20 comprises a structural body 24 that is shaped as a ring 25, as schematically illustrated in FIG. 2. The ring 25 comprises the surface 26 having the microcracks 28. The ring 25 is annular with an internal sidewall 28 and an external sidewall 30. The internal sidewall 28 faces an internal axis 34 about which the structural body has rotational symmetry. The ring 25 is shaped to protect or conform to a section of a processing chamber, chamber component, or substrate within the chamber. For example, the component 20 can be a liner or shield that is a cylindrical member which is sized to fit around a substrate being processed in a chamber. The shield 20 can be a rig of quartz that surrounds the substrate. The component 20 can also be a deposition ring, shadow ring or cover ring. Yet other chamber components comprise chamber wall liners.


The surface microcracks 28 on the structural body 24 of the component 20 are annealed to heal and close off the microcracks as shown in FIGS. 1B and 1D, to reduce crack propagation and increase the fracture resistance of the component 20. In one embodiment, a laser beam is directed onto the localized surface regions 26 of the component 20 at a sufficiently high intensity and for a sufficient time to cause the region 26 about the microcracks 28 to soften and heal the microcracks 28. The laser beam is used to selectively heat the localized surface regions of the component 20. The localized surface regions 26 are those that are prone to fracture during use, or which have excessive microcracks during fabrication, for example, regions which are more readily subject to abrasion and grinding from applied external forces during the handling of manufacture of the component. Thus, the localized surface regions may be on the flat top surface of the ring 25. The localized surface regions 26 can also include those regions of the component 20 which are more susceptible to applied stresses during handling and use. For example, the edges 36 of the quartz rings 25 used in the chamber 20 are often chipped or cracked when the ring 25 is removed for cleaning or replacing after use for a predetermined number of process cycles. The edges 36, which may also include corners 40, are often easily cracked or chipped in use. Thus, increasing the fracture strength of the regions 26 of the quartz ring can significantly increase its process lifetime.


The energy of the laser beam and beam characteristics, such as focal length, beam shape and beam diameter, may be controlled to selectively heat a shallow portion of the localized surface region of the component 20 above the microcrack healing temperature needed for annealing the surface microcracks 28. In one embodiment, a laser beam is used to heat a thin surface layer having a depth of less than 500 microns, and more typically less the 100 microns, of the localized surface regions 26 of a component 20. The focused laser beam selectively heats the localized surface regions 26 of the component 20 to a temperature above the crack healing temperature without excessively raising the bulk temperature of the component, which may result in distortion or thermal fracture of the component 20. After heating the thin surface layer of the component 20, rapid quenching of the hot surface occurs simply by conduction of heat out of the surface into the ambient environment. Since only a very shallow portion of the localized surface region 26 is heated by the laser beam, the quench rate by natural conduction or convection is relatively fast.


While a laser beam heat treatment is described as an exemplary annealing process, other annealing processes can also be used. For example, alternative annealing processes include plasma jet heating, electrical arc heating, flame heating. Thus, the scope of the present invention should not be limited to the exemplary versions described herein, and the invention includes other localized surface annealing processes and apparatus as would be apparent to those of ordinary skill in the art.


The microcrack formation process is essentially partially or entirely reversed by the annealing step. The localized heat energy supplied to the microcracked surface by the laser causes softening and fluxing of the localized heated region causing the microcracks 28 to close and seal themselves off, as schematically shown in FIGS. 1B and 1D. It is believed that in amorphous or glassy materials, as shown in FIGS. 1A and 1B, the microcrack healing process is enhanced because atomic forces acting across the tips of the microcracks 28 tend to pull crack surfaces back into contact across the entire microcrack plane. In microcrystalline materials, as shown in FIGS. 1C and 1D, the grain boundary regions 31 often contain small amounts of impurities that act as fluxing agents causing more rapid fluxing and resultant healing of the microcrack surfaces.


The effects of the laser annealing treatment are shown in FIGS. 3A and 3B, which are optical microscopy images of a quartz surface comprising surface microcracks before and after laser treatment, respectively. FIG. 3A shows the quartz surface with a large number of microcracks corresponding to the dark lines between the lighter grain surface regions. In FIG. 3B, which is a photo of the laser treated sample, it is seen that most of the surface microcracks have disappeared to provide a smooth and continuous surface. Note also that an indentation mark was artificially made at the center of the quartz specimen. However, the size of the indentation mark was on the order of the surface roughness of the quartz material, consequently, it is not visible in the original, un-treated quartz material shown in FIG. 3A. However, the partially healed indentation mark is visible as a faint dark spot in the photo of the laser treated sample of FIG. 3B, because the surface of the laser treated specimen is smooth and absent surface microcracks and roughness.


Annealing of surface microcracks of the chamber components was also found to substantially increase hardness and fracture stress of the annealed material, which would significantly improve its resistance to chipping and cracking. In the hardness test, an increasing load was applied normal to the plane of the specimen surface using a micro-indenter having a known geometrical shape. The load is then reduced until the surface of the specimen partially or completely relaxes, and a depth of indentation is then measured. The load is then progressively increased and the indentation and measurement process repeated until hardness is compromised and the specimen cracks. The Vickers hardness is computed using the formula H=Pmax/Ac, where Pmax is the maximum load sustained before cracking and Ac is the projected area of contact of the indenter. The hardness was measured using a Nano Hardness Tester. The load applied was on the order of a nano Newton and the displacement was accurately determined using a differential capacitor sensor. Both an original untreated quartz specimen and a laser annealed quartz specimen were measured. The mean Vickers hardness index for the untreated specimen was about 771.68, and the Vickers hardness index for the laser annealed quartz specimen had a mean of 951.68. Thus, the laser annealed quartz specimen had a Vickers hardness which was at least about 10%, and more preferably at least about 25% harder than the untreated specimen.


Another measurement demonstrating increased crack and chip resistance is a fracture stress measurement. Ceramic materials are often tested in a flexural or bending test instead of tensile test because of their brittle nature. The stress at which the ceramic material fails by fracture is called the fracture stress or fracture strength of the material. The fracture stress of untreated and laser annealed quartz specimens were compared from a 4-point bending test performed on the Universal Testing Machine according to ASTM C1161-90. The load at fracture and a cross-sectional area of the specimen was used to compute the stress fracture from the formula σ=Load/wxt, where wxt is cross sectional area over which the load is applied. The mean fracture stress of the untreated quartz specimens was 86.23 MPa and the mean fracture stress of the laser annealing quartz specimen was 132.27 MPa. Thus, the mean fracture stress of the laser annealed quartz specimen was at least about 25%, and more preferably, at least about 50% higher than that of the untreated specimen.


Thus, annealing of the microcracks 28 in localized surface regions 26 of a component 20 can significantly increase the surface smoothness, hardness, and fracture strength of the component 20. Absence or reduction of microcracks 28 in the surface of the component 20, especially in regions which are susceptible to applied stresses or are simply more fragile, such as projections, corners 40 and edges of the component, substantially increases the crack and chip resistance of the component 20. Advantageously, surface annealing allows healing and increased strength of selected surface regions 26 without subjecting the entire component 20 to elevated temperatures that may cause structural deformation or other thermal degradation. However, the entire component may also be annealed by suitable heat treatment.


Annealing of the microcracks 28 in localized surface regions 26 of the component 20 can be performed using a laser annealing apparatus 50, an exemplary embodiment of which is shown in FIG. 4. The laser annealing apparatus 50 comprises a laser beam enclosure 52 that encloses a laser beam source 54 powered by a power supply 55. Suitable laser beam sources 54 that can be used for microcrack annealing include, for example, Ar (argon), CO2 and KrF lasers. An argon laser transmits in the visible wavelength at about 5145 angstroms. A CO2 laser is an infra-red energy source having a wavelength of 10.6 μm, and can provide beams having a power of the order of 10 kilowatts. The CO2 laser is 100× more efficient than the argon laser and is of greater intensity, allowing much faster scan speeds and larger spot sizes than the argon laser. A CO2 laser is described in U.S. Pat. No. 3,702,973 issued on Nov. 14, 1972, which is incorporated herein in its entirety. Yet another type of laser is a KrF excimer laser having a wavelength of about 248 nm, an Eg of 5.0 eV, an efficiency of about 3%, and an output energy of 350 mJ. The laser beam is typically a circular beam having a beam diameter of typically less than about 10 mm, and more typically from about 0.5 mm to about 4 mm. Thus, suitable laser beams can have wavelengths of from about 190 nm to about 10,600 nm. The laser is typically operated at a power level of from about 5 Watts to about 10,000 Watts.


The laser 50 produces a laser beam 56 that is focused at a primary focal point 58 and is re-imaged by a refocusing mirror 62 which provides a larger focal length, to a secondary focal point 84. Between the refocusing mirror 62 and the secondary focal point 84 is the dithering mirror 68 which is connected to a dithering drive motor 72 which vibrates the dithering mirror 68 at a preselected frequency. The dithering drive motor 72 vibrates the dithering mirror 68 about an axis 76 substantially in the plane of the mirror 68 and transverse to the incident laser beam 56 focused by mirror. The dithered beam emanating from the dithering mirror 68 spacially oscillates an arc line which is transverse to the plane of the drawing in FIG. 1.


Typically, the laser beam 56 has an intensity distribution across the beam diameter, also called the intensity profile or intensity shape of the beam, which depends on the type of laser 50. A common beam profile shape is a Gaussian shape, and more typically a U-shaped intensity profile. Focusing of the laser beam changes the cross-sectional size of the beam but not its beam intensity distribution which remains Gaussian or U-shaped. One method of correcting for the Gaussian or U-shaped cross-section of the laser beam is to spacially oscillate the laser beam 56, also known as dithering. The spacial oscillation of the laser beam 56 may be sinusoidal, sawtooth or square waves. Spacial oscillation or dithering of the laser beam 56 produces an average and more uniform intensity of radiation across the region scanned by the dithering beam. In one embodiment, the laser beam 56 has an approximate Gaussian distribution at its focal point and the spacial oscillation or dithering is sinusoidal. The dithering is produced by the dithering mirror 76 which oscillates back and forth on the axis 76 that is parallel to the plane of the mirror 76 and transverse to the plane of the dither. Typically, the dithered beam covers an area that at least twice as large as the undithered beam. For sinusoidal dithering, the average intensity at each point across the dithering beam projected on the localized surface region is approximately flat in the center region and with peaks at the opposite ends. The resulting intensity profile of the dithering beam is shaped like a square wave and provides a good intensity profile for scanning across the localized surface region in contiguous, overlapping sweeps. however, other beam shapes, such as sine wave shapes, can also be used with appropriately compensating laser scanning methods.


The dithered beam then passes through a beam width controlling aperture 80 having a controllable or predefined fixed aperture 82 at the second focal point 84. The aperture 80 is located between the dithering mirror 76 and a second focusing system 90 which may be a scanning mirror or lens. The axis 76 of mirror 68 may be transverse or parallel to the plane of the drawing in FIG. 1. The beam is then projected onto a scanning mirror 92 driven by a scanning system 94. The scanning system 94 oscillates the mirror 92 on its axis 96 to sweep and scan the beam 56 back and forth over a selected localized region 100 on the chamber component being treated. The scanned beam passes through a window 102 in the enclosure 100. The sweep rate of scanning mirror 92 is typically slower than the dither frequency of the dithering mirror 68. For example, a focused CO2 laser having a beam diameter of about 500 μm may be scanned at from about 1 mm/sec to about 100 mm/sec.


The scanning system communicates with an X-Y movable stage 110 which is driven by a stage motor 114. The stage 110 can also be adapted to slide in the Z or vertical direction to change the beam width incident on the component. The scanning system 94 synchronizes the sweep rate of the scanning mirror 92 with the movement of the stage 110, and consequently, the movement of the chamber component resting on the stage 110, to uniformly scan the dithered and apertured beam across the component. The scanning parameters are selected to uniformly heat the localized surface region across which the beam is being scanned, by adjusting the scanning speed and pattern to compensate for the shape of the laser beam. For example, the intensity distribution of the beam 56 can contain rings around a central maximum and even a depression in the middle of the beam due to near field annular characteristics of the beam. Furthermore, it is also desirable to overlap the beam scans to compensate for any variation in the cross-sectional intensity of a laser beam—if the laser beam sweeps across the surface in raster-type scans without overlapping of beam scans, the depth of heat treatment may vary across the beam scan depending on the shape of the beam.


The laser beam annealing apparatus 50 further comprises a controller 118 which controls operation of the system and is connected to the power supply 55, which powers the laser 54, the dithering drive motor 72, and the scanning system 94. In addition, the controller 118 accepts input from a user input device 120 and displays input parameters, and scanning system information on a display 122. The controller 118 can be a conventional computer having a central processing unit (CPU) connected to suitable memory devices, including random access memory and storage memory on disk drives, and interface cards and buses. The laser beam annealing apparatus 50 is capable of laser annealing localized surface regions across the component surface with good uniformity over the entire surface region.


A component 20 that is annealed to reduce or heal microcracks can be used in a substrate processing apparatus 200, as schematically illustrated in FIG. 5, which is used to fabricate substrates 215, such as semiconductor wafers and displays. The apparatus 200 can be a MxP, MxP Super E, or eMax type etching chamber, which are from Applied Materials Inc., Santa Clara, Calif., and are generally described in commonly assigned U.S. Pat. Nos. 4,842,683 and 5,215,619 to Cheng et al; and U.S. Pat. No. 4,668,338 to Maydan et al, all of which are incorporated herein by reference in their entireties. An exemplary apparatus 200 may be used in a multi-chamber integrated system for processing semiconductor substrates as described in U.S. Pat. No. 4,951,601 to Maydan et al, which is also incorporated herein by reference in its entirety.


Generally, the apparatus 200 comprises a process chamber 225 and ancillary control, electrical, plumbing and support components. A support assembly 230 comprising a support 238 is provided to receive the substrate 215 in a process zone 235. The support 238 may be an electrostatic chuck 240 comprising a dielectric 45 at least partially covering an electrode 250, and having gas outlets 260 through which a heat transfer gas, such as helium, may be passed from a heat transfer gas source 265 via gas conduits 270, to control the temperature of the substrate 215. Alternatively, the support 238 may be a vacuum or mechanical chuck or any other support as is known in the art. The electrode 250 is electrically charged by an electrode voltage supply 275 to electrostatically hold the substrate 215. A base 280 below the electrostatic chuck 240 may optionally contain a heat exchanger, such as channels through which a heat transfer fluid may be circulated.


Process gas is introduced into the chamber 225 through a gas supply 285 that includes a gas source 290 and one or more gas nozzles 295 terminating in the chamber 225. The gas nozzles 295 may be located around the periphery of the substrate 215 (as shown) or in a showerhead mounted on the ceiling of the chamber (not shown). A gas flow controller 300 is used to control the flow rate of the process gas. Spent process gas and byproducts are exhausted from the chamber 225 through an exhaust system 305. The exhaust system 305 typically comprises an exhaust conduit leading to a plurality of pumps, such as roughing or high vacuum pumps, that evacuate the gas in the chamber 225. A throttle valve 310 is provided in the exhaust conduit to control the pressure of the gas in the chamber 225.


An energized gas, such as for example a gaseous plasma, is generated from the process gas by a gas energizer 275 that couples electromagnetic energy, such as RF or microwave energy, to the process gas in the process zone 235 of the chamber 225. For example, the gas energizer 275 may comprise a first process electrode 315 such as an electrically grounded sidewall or ceiling of the chamber and a second electrode which may be the electrode 250 in dielectric 245. The first and second electrodes 315, 250 are electrically biased relative to one another by an RF voltage provided by an electrode voltage supply 275. The frequency of the RF voltage applied to the electrodes 315, 250 is typically from about 50 KHz to about 60 MHz. In other versions, the gas energizer 275 may also or alternatively include an inductor antenna (not shown) comprising one or more coils to inductively couple RF energy to the chamber 225. The capacitively generated plasma may be enhanced by electron cyclotron resonance in a magnetically enhanced reactor in which a magnetic field generator 320, such as a permanent magnet or electromagnetic coils, provides a magnetic field in the chamber 225 that has a rotating magnetic field having an axis that rotates parallel to the plane of the substrate 215.


The chamber 225 may also comprise one or more process monitoring systems (not shown) to monitor the processes being performed on the substrate 215. A typical process monitoring system comprises an interferometric system that measures an intensity of light reflected from a layer being processed on the substrate 215, or a plasma emission analysis system that measures a change in light emission intensity of a gas species in the chamber 225. The process monitoring system is useful to detect an endpoint of a process being performed on the substrate 215.


The laser annealed component 20 such as the ring 25 is fitted around the substrate support 238 of the support assembly 230 in the chamber 225. The ring 25 may protect the support assembly 230, for example, the dielectric 245 of the electrostatic chuck 240 from erosion by preventing contact of the dielectric 245 with the energized process gas in the chamber 225. Alternatively, the ring 25 may have other uses in the support assembly 230.


Referring to FIG. 6, additional structures, such as the collar 210 which surrounds the ring 25 can also be laser annealed to reduce surface microcracks. The collar 210 can be made from a ceramic material such as aluminum oxide or silicon oxide. The collar 210 may serve as a shield, which together with the ring form a replaceable process kit for the chamber. Other annular structures such as chamber wall liners can also be laser annealed, and can also be part of the process kit for the chamber 225.


Although exemplary embodiments of the present invention are shown and described, those of ordinary skill in the art may devise other embodiments which incorporate the present invention, and which are also within the scope of the present invention. For example, the annealed chamber component 20 can be from chamber components such as the ceiling or walls of the chamber 225. In addition, alternative methods of surface annealing can also be used. Furthermore, relative or positional terms shown with respect to the exemplary embodiments are interchangeable. Therefore, the appended claims should not be limited to the descriptions of the preferred versions, materials, or spatial arrangements described herein to illustrate the invention.

Claims
  • 1. A substrate processing chamber component comprising: (a) a processing chamber component structural body comprising a substrate support, gas distributor, gas energizer, collar, ring, shield, ceiling, wall, or liner; and(b) localized surface regions on the structural body, the localized surface regions comprising (i) annealed microcracks having crack surfaces that are in contact with one another, and (ii) a mean Vickers hardness that is at least about 10% higher than the Vickers hardness of the untreated structural body.
  • 2. A component according to claim 1 comprising localized surface regions with laser-annealed microcracks.
  • 3. A component according to claim 1 comprising localized surface regions with CO2 laser-annealed microcracks.
  • 4. A component according to claim 1 wherein the structural body has rotational symmetry about an internal axis.
  • 5. A component according to claim 1 wherein the structural body is made from a ceramic, glass or glass-ceramic.
  • 6. A component according to claim 1 wherein the structural body comprises quartz.
  • 7. A component according to claim 1 wherein the localized surface regions are surfaces or edges of the structural body.
  • 8. A component according to claim 1 wherein the component comprises a mean fracture stress that is at least about 25% higher than the untreated structural body.
  • 9. A component according to claim 1 wherein the structural body comprises a ring.
  • 10. A component according to claim 1 wherein the structural body comprises a plate.
  • 11. A component according to claim 1 wherein the structural body comprises a cylinder.
  • 12. A component according to claim 1 wherein the crack surfaces are in contact across the entire microcrack plane.
  • 13. A component according to claim 1 wherein the localized surface regions consist essentially of the annealed microcracks.
  • 14. A component according to claim 1 wherein the component is a substrate support, a gas distributor, a gas energizer, a focus ring, a deposition ring, a substrate shield or a chamber wall liner.
  • 15. A substrate processing chamber comprising at least one substrate processing chamber component according to claim 1.
  • 16. A substrate processing chamber component comprising: a processing chamber component structural body having a shape that is adapated for use in a substrate processing chamber and localized surface regions comprising (i) annealed microcracks that are healed and closed off such that the crack surfaces of the annealed microcracks are in contact across the entire microcrack plane, and (ii) a mean Vickers hardness that is at least about 10% higher than the Vickers hardness of the untreated structural body.
  • 17. A component according to claim 16 comprising localized surface regions with laser-annealed microcracks.
  • 18. A component according to claim 16 wherein the laser microcracks are CO2 laser-annealed microcracks.
  • 19. A component according to claim 16 wherein the structural body comprises a ring, plate or cylinder.
  • 20. A component according to claim 16 wherein the structural body is made from ceramic, glass or glass-ceramic.
  • 21. A component according to claim 16 wherein the structural body comprises quartz.
  • 22. A component according to claim 16 wherein the localized surface regions are surfaces or edges of the structural body.
  • 23. A component according to claim 16 wherein the component comprises a mean fracture stress that is at least about 25% higher than the untreated structural body.
  • 24. A component according to claim 16 wherein the annealed microcracks are healed and closed off by themselves.
  • 25. A component according to claim 16 wherein the component is substrate support, a gas distributor, a gas energizer, a focus ring, a deposition ring, a substrate shield or a chamber wall liner.
  • 26. A substrate processing chamber comprising at least one substrate processing chamber component according to claim 16.
  • 27. A substrate processing chamber component comprising: a processing chamber component structural body having a shape that is adapted for use in a substrate processing chamber and localized surface regions (i) consisting essentially of annealed microcracks that are healed and closed off by themselves, and wherein the crack surfaces of teh annealed microtracks are in contact across the entire microtrack plane, and (ii) having a mean Vickers hardness that is at least about 10% higher than the Vickers hardness of the untreated surface.
  • 28. A component according to claim 27 wherein the structural body comprises a ring, plate or cylinder.
  • 29. A component according to claim 28 wherein the structural body is made from ceramic, glass or glass-ceramic.
  • 30. A component according to claim 28 wherein the structural body comprises quartz.
  • 31. A component according to claim 27 wherein the component is a substrate support, a gas distributor, a gas energizer, a focus ring, a deposition ring, a substrate shield or a chamber wall liner.
  • 32. A substrate processing chamber comprising at least one substrate processing chamber component according to claim 27.
US Referenced Citations (425)
Number Name Date Kind
2705500 Deer Apr 1955 A
3117883 Pierett Jan 1964 A
3457151 Kortejarvi Jul 1969 A
3482082 Israeli Dec 1969 A
3522083 Woolman Jul 1970 A
3565771 Gulla Feb 1971 A
3679460 Reid Jul 1972 A
3843472 Toussaint et al. Oct 1974 A
3848104 Locke Nov 1974 A
4358659 Spohnheimer Nov 1982 A
RE31198 Binns Apr 1983 E
4412133 Eckes et al. Oct 1983 A
4419201 Levinstein et al. Dec 1983 A
4430360 Bill et al. Feb 1984 A
4480284 Tojo et al. Oct 1984 A
4491496 Laporte et al. Jan 1985 A
4606802 Kobayashi et al. Aug 1986 A
4643950 Ogura et al. Feb 1987 A
4645218 Ooshio et al. Feb 1987 A
4665463 Ward et al. May 1987 A
4673554 Niwa et al. Jun 1987 A
4713119 Earhart et al. Dec 1987 A
4717462 Homma et al. Jan 1988 A
4732792 Fujiyama Mar 1988 A
4756322 Lami Jul 1988 A
4814575 Petitbon Mar 1989 A
4832781 Mears May 1989 A
4872250 De Marco Oct 1989 A
4913784 Bogenshutz et al. Apr 1990 A
4959105 Neidiffer et al. Sep 1990 A
4995958 Anderson et al. Feb 1991 A
4996859 Rose et al. Mar 1991 A
5009966 Garg et al. Apr 1991 A
5032469 Merz et al. Jul 1991 A
5035787 Parker et al. Jul 1991 A
5055964 Logan et al. Oct 1991 A
5064511 Gobbetti et al. Nov 1991 A
5104501 Okabayashi Apr 1992 A
5104834 Watanabe et al. Apr 1992 A
5117121 Watanabe et al. May 1992 A
5151845 Watanabe et al. Sep 1992 A
5164016 Henriet et al. Nov 1992 A
5166856 Liporace et al. Nov 1992 A
5180322 Yamamoto et al. Jan 1993 A
5180563 Lai et al. Jan 1993 A
5191506 Logan et al. Mar 1993 A
5202008 Talieh Apr 1993 A
5215624 Dastolfo et al. Jun 1993 A
5215639 Boys Jun 1993 A
5242706 Cotell et al. Sep 1993 A
5248386 Dastolfo et al. Sep 1993 A
5258047 Tokisue et al. Nov 1993 A
5270266 Hirano et al. Dec 1993 A
5275683 Arami et al. Jan 1994 A
5280156 Niori et al. Jan 1994 A
5292554 Sinha et al. Mar 1994 A
5304248 Cheng et al. Apr 1994 A
5314597 Harra May 1994 A
5315473 Collins et al. May 1994 A
5324053 Kubota et al. Jun 1994 A
5325261 Horwitz Jun 1994 A
5338367 Henriet et al. Aug 1994 A
5350479 Collins et al. Sep 1994 A
5356723 Kimoto et al. Oct 1994 A
5366585 Robertson et al. Nov 1994 A
5382469 Kubota et al. Jan 1995 A
5391275 Mintz Feb 1995 A
5401319 Banholzer et al. Mar 1995 A
5407551 Sieck et al. Apr 1995 A
5409590 Hurwitt et al. Apr 1995 A
5427825 Murnick Jun 1995 A
5429711 Watanabe et al. Jul 1995 A
5433835 Demaray et al. Jul 1995 A
5458759 Hosokawa et al. Oct 1995 A
5460694 Schapira et al. Oct 1995 A
5463526 Mundt Oct 1995 A
5474649 Kava et al. Dec 1995 A
5487822 Demaray et al. Jan 1996 A
5490913 Schertler et al. Feb 1996 A
5509558 Imai et al. Apr 1996 A
5512078 Griffin Apr 1996 A
5518593 Hoskawa et al. May 1996 A
5520740 Kanai et al. May 1996 A
5531835 Fodor et al. Jul 1996 A
5542559 Kawakami et al. Aug 1996 A
5549802 Guo Aug 1996 A
5587039 Salimian et al. Dec 1996 A
5595583 Murnick Jan 1997 A
5605637 Shan et al. Feb 1997 A
5614055 Fairbairn et al. Mar 1997 A
5614071 Mahvan et al. Mar 1997 A
5643422 Yamada Jul 1997 A
5658442 Van Gogh et al. Aug 1997 A
5660640 Laube Aug 1997 A
5671835 Tanaka et al. Sep 1997 A
5684669 Collins et al. Nov 1997 A
5685914 Hills et al. Nov 1997 A
5685959 Bourez et al. Nov 1997 A
5690795 Rosenstein et al. Nov 1997 A
5695825 Scruggs Dec 1997 A
5700179 Hasegawa et al. Dec 1997 A
5714010 Matsuyama et al. Feb 1998 A
5720818 Donde et al. Feb 1998 A
5736021 Ding et al. Apr 1998 A
5745331 Shamouilian et al. Apr 1998 A
5748434 Rossman et al. May 1998 A
5755887 Sano et al. May 1998 A
5762748 Banholzer et al. Jun 1998 A
5763851 Forster et al. Jun 1998 A
5792562 Collins et al. Aug 1998 A
5800686 Littau et al. Sep 1998 A
5803977 Tepman et al. Sep 1998 A
5808270 Marantz et al. Sep 1998 A
5810931 Stevens et al. Sep 1998 A
5812362 Ravi Sep 1998 A
5821166 Hajime et al. Oct 1998 A
5824197 Tanaka Oct 1998 A
5830327 Kolnekow Nov 1998 A
5840434 Kojima et al. Nov 1998 A
5855687 DuBois et al. Jan 1999 A
5858100 Maeda et al. Jan 1999 A
5868847 Chen et al. Feb 1999 A
5876573 Moslehi et al. Mar 1999 A
5879523 Wang et al. Mar 1999 A
5879524 Hurwitt et al. Mar 1999 A
5885428 Kogan Mar 1999 A
5886863 Nagasaki et al. Mar 1999 A
5893643 Kumar et al. Apr 1999 A
5901751 Huo May 1999 A
5903428 Grimard et al. May 1999 A
5910338 Donde et al. Jun 1999 A
5916378 Bailey et al. Jun 1999 A
5916454 Richardson et al. Jun 1999 A
5920764 Hanson Jul 1999 A
5922133 Tepman et al. Jul 1999 A
5930661 Lu Jul 1999 A
5939146 Lavernia Aug 1999 A
5942041 Lo et al. Aug 1999 A
5942445 Kato et al. Aug 1999 A
5948288 Treves et al. Sep 1999 A
5951374 Kato et al. Sep 1999 A
5951775 Tepman Sep 1999 A
5953827 Or et al. Sep 1999 A
5963778 Stellrecht Oct 1999 A
5967047 Kuhn et al. Oct 1999 A
5976327 Tanaka Nov 1999 A
5985033 Yudovsky et al. Nov 1999 A
6000415 Huo et al. Dec 1999 A
6010583 Annavarapu et al. Jan 2000 A
6014979 Van Autryve et al. Jan 2000 A
6015465 Kholodenko et al. Jan 2000 A
6026666 Zimmermann et al. Feb 2000 A
6027604 Lim et al. Feb 2000 A
6036587 Tolles et al. Mar 2000 A
6051114 Yao et al. Apr 2000 A
6051122 Flanigan Apr 2000 A
6059945 Fu et al. May 2000 A
6071389 Zhang Jun 2000 A
6073830 Hunt et al. Jun 2000 A
6086735 Gilman et al. Jul 2000 A
6095084 Shamouilian et al. Aug 2000 A
6096135 Guo et al. Aug 2000 A
6103069 Davenport Aug 2000 A
6103070 Hong Aug 2000 A
6106625 Koai et al. Aug 2000 A
6108189 Weldon et al. Aug 2000 A
6120621 Jin et al. Sep 2000 A
6120640 Shih et al. Sep 2000 A
6123804 Babassi et al. Sep 2000 A
6132566 Hofmann et al. Oct 2000 A
6143086 Tepman Nov 2000 A
6143432 de Rochemont et al. Nov 2000 A
6146509 Aragon Nov 2000 A
6149784 Su et al. Nov 2000 A
6150762 Kim et al. Nov 2000 A
6152071 Akiyama et al. Nov 2000 A
6156124 Tobin Dec 2000 A
6159299 Koai et al. Dec 2000 A
6162297 Mintz et al. Dec 2000 A
6162336 Lee Dec 2000 A
6168668 Yudovsky Jan 2001 B1
6170429 Schoepp et al. Jan 2001 B1
6176981 Hong et al. Jan 2001 B1
6183614 Fu Feb 2001 B1
6183686 Bardus et al. Feb 2001 B1
6190513 Forster et al. Feb 2001 B1
6190516 Xiong et al. Feb 2001 B1
6198067 Ikeda et al. Mar 2001 B1
6199259 Demaray et al. Mar 2001 B1
6210539 Tanaka et al. Apr 2001 B1
6221217 Moslehi et al. Apr 2001 B1
6227435 Lazarz et al. May 2001 B1
6235163 Angelo et al. May 2001 B1
6238528 Xu et al. May 2001 B1
6248667 Kim et al. Jun 2001 B1
6250251 Akiyama et al. Jun 2001 B1
6251720 Thakur et al. Jun 2001 B1
6254737 Edelstein et al. Jul 2001 B1
6258170 Somekh et al. Jul 2001 B1
6258440 Aihara et al. Jul 2001 B1
6264812 Raaijmakers et al. Jul 2001 B1
6269670 Koestermeier Aug 2001 B2
6270859 Zhao et al. Aug 2001 B2
6274008 Gopalraja et al. Aug 2001 B1
6276997 Li Aug 2001 B1
6280584 Kumar et al. Aug 2001 B1
6284093 Ke et al. Sep 2001 B1
6287437 Pandhumsoporn et al. Sep 2001 B1
6299740 Hieronymi et al. Oct 2001 B1
6306489 Hellmann et al. Oct 2001 B1
6306498 Yuuki et al. Oct 2001 B1
6328808 Tsai et al. Dec 2001 B1
6338781 Sichmann et al. Jan 2002 B1
6338906 Ritland et al. Jan 2002 B1
6340415 Raaijmakers et al. Jan 2002 B1
6344114 Sichmann et al. Feb 2002 B1
6346352 Hayden et al. Feb 2002 B1
6358376 Wang et al. Mar 2002 B1
6364957 Schneider et al. Apr 2002 B1
6365010 Hollars Apr 2002 B1
6368469 Nulman et al. Apr 2002 B1
6372609 Aga Apr 2002 B1
6374512 Guo et al. Apr 2002 B1
6379575 Yin et al. Apr 2002 B1
6383459 Singh et al. May 2002 B1
6387809 Toyama May 2002 B2
6391146 Bhatnagar et al. May 2002 B1
6394023 Crocker May 2002 B1
6398929 Chiang et al. Jun 2002 B1
6401652 Mohn et al. Jun 2002 B1
6416634 Mostovoy et al. Jul 2002 B1
6423175 Huang et al. Jul 2002 B1
6432203 Black et al. Aug 2002 B1
6436192 Chen et al. Aug 2002 B2
6440221 Shamouilian et al. Aug 2002 B2
6444083 Steger et al. Sep 2002 B1
6447853 Suzuki et al. Sep 2002 B1
6454870 Brooks Sep 2002 B1
6484794 Park et al. Oct 2002 B1
6475336 Hubacek Nov 2002 B1
6486020 Thakur et al. Nov 2002 B1
6497797 Kim Dec 2002 B1
6500321 Ashtiani et al. Dec 2002 B1
6503331 Yudovsky et al. Jan 2003 B1
6506290 Ono Jan 2003 B1
6506312 Bottomfield Jan 2003 B1
6544914 Kikugawa et al. Apr 2003 B1
6545267 Miura et al. Apr 2003 B1
6555471 Sandhu et al. Apr 2003 B2
6558505 Suzuki et al. May 2003 B2
6565984 Wu et al. May 2003 B1
6566161 Rosenberg et al. May 2003 B1
6572732 Collins Jun 2003 B2
6576909 Donaldson et al. Jun 2003 B2
6579431 Bolcavage et al. Jun 2003 B1
6589407 Subramani et al. Jul 2003 B1
6599405 Hunt et al. Jul 2003 B2
6605177 Mett et al. Aug 2003 B2
6619537 Zhang et al. Sep 2003 B1
6620736 Drewery Sep 2003 B2
6623595 Han et al. Sep 2003 B1
6623596 Collins et al. Sep 2003 B1
6623597 Han et al. Sep 2003 B1
6623610 Onishi Sep 2003 B1
6627050 Miller et al. Sep 2003 B2
6627056 Wang et al. Sep 2003 B2
H2087 Balliett et al. Nov 2003 H
6645357 Powell Nov 2003 B2
6652668 Perry et al. Nov 2003 B1
6652716 Kao et al. Nov 2003 B2
6660135 Yu et al. Dec 2003 B2
6667577 Shannon et al. Dec 2003 B2
6673199 Yamartino et al. Jan 2004 B1
6676812 Chung Jan 2004 B2
6682627 Shamouilian et al. Jan 2004 B2
6689249 Ke et al. Feb 2004 B2
6689252 Shamouilian et al. Feb 2004 B1
6708870 Koenigsmann et al. Mar 2004 B2
6723214 Stimson et al. Apr 2004 B2
6726805 Brown et al. Apr 2004 B2
6730174 Liu et al. May 2004 B2
6743340 Fu Jun 2004 B2
6749103 Ivanov et al. Jun 2004 B1
6776879 Yamamoto et al. Aug 2004 B2
6777045 Lin et al. Aug 2004 B2
6783639 Nulman et al. Aug 2004 B2
6794703 Thakur et al. Sep 2004 B1
6797362 Parfeniuk et al. Sep 2004 B2
6797639 Carducci et al. Sep 2004 B2
6811657 Jaso Nov 2004 B2
6812471 Popiolkowski et al. Nov 2004 B2
6824612 Stevens et al. Nov 2004 B2
6824652 Park Nov 2004 B2
6837968 Brown et al. Jan 2005 B2
6840427 Ivanov Jan 2005 B2
6846396 Perrin Jan 2005 B2
6858116 Okabe et al. Feb 2005 B2
6872284 Ivanov et al. Mar 2005 B2
6902627 Brueckner et al. Jun 2005 B2
6902628 Wang et al. Jun 2005 B2
6916407 Vosser et al. Jul 2005 B2
6933025 Lin et al. Aug 2005 B2
6933508 Popiolkowski et al. Aug 2005 B2
6942929 Han et al. Sep 2005 B2
6955748 Kim Oct 2005 B2
6955852 Ivanov Oct 2005 B2
6992261 Kachalov et al. Jan 2006 B2
7026009 Lin et al. Apr 2006 B2
7041200 Le et al. May 2006 B2
7049612 Quach et al. May 2006 B2
7063773 Ivanov et al. Jun 2006 B2
7097744 Liu et al. Aug 2006 B2
7121938 Suzuki Oct 2006 B2
7131883 Park et al. Nov 2006 B2
7141138 Gondhalekar et al. Nov 2006 B2
7146703 Ivanov Dec 2006 B2
7223323 Yang et al. May 2007 B2
7264679 Schweitzer et al. Sep 2007 B2
7294224 Vesci et al. Nov 2007 B2
7294245 Fu Nov 2007 B2
7407565 Wang et al. Aug 2008 B2
7504008 Doan et al. Mar 2009 B2
7579067 Lin et al. Aug 2009 B2
7604708 Wood et al. Oct 2009 B2
7618769 Brueckner et al. Nov 2009 B2
20010001367 Koestermeier May 2001 A1
20010033706 Shimomura et al. Oct 2001 A1
20010045353 Hieronymi et al. Nov 2001 A1
20020029745 Nagaiwa et al. Mar 2002 A1
20020033330 Demaray et al. Mar 2002 A1
20020066531 Ke et al. Jun 2002 A1
20020076490 Chiang et al. Jun 2002 A1
20020086118 Chang et al. Jul 2002 A1
20020090464 Jiang et al. Jul 2002 A1
20020092618 Collins Jul 2002 A1
20020100680 Yamamoto et al. Aug 2002 A1
20030000647 Yudovsky Jan 2003 A1
20030006008 Horioka et al. Jan 2003 A1
20030019746 Ford et al. Jan 2003 A1
20030026917 Lin et al. Feb 2003 A1
20030029568 Brown et al. Feb 2003 A1
20030037883 Mett et al. Feb 2003 A1
20030047464 Sun et al. Mar 2003 A1
20030077199 Sandlin et al. Apr 2003 A1
20030085121 Powell May 2003 A1
20030108680 Gell et al. Jun 2003 A1
20030116276 Weldon et al. Jun 2003 A1
20030118731 He et al. Jun 2003 A1
20030127049 Han et al. Jul 2003 A1
20030127319 Demaray et al. Jul 2003 A1
20030136428 Krogh Jul 2003 A1
20030168168 Liu et al. Sep 2003 A1
20030170486 Austin et al. Sep 2003 A1
20030173526 Popiolkowski et al. Sep 2003 A1
20030185965 Lin et al. Oct 2003 A1
20030188685 Wang et al. Oct 2003 A1
20030196890 Le et al. Oct 2003 A1
20030217693 Rattner et al. Nov 2003 A1
20030218054 Koenigsmann et al. Nov 2003 A1
20030221702 Peebles Dec 2003 A1
20040016637 Yang et al. Jan 2004 A1
20040026233 Perrin Feb 2004 A1
20040031677 Wang et al. Feb 2004 A1
20040045574 Tan Mar 2004 A1
20040056070 Ivanov Mar 2004 A1
20040056211 Popiolkowski et al. Mar 2004 A1
20040079634 Wickersham et al. Apr 2004 A1
20040083977 Brown et al. May 2004 A1
20040099285 Wang et al. May 2004 A1
20040113364 Ivanov Jun 2004 A1
20040118521 Pancham et al. Jun 2004 A1
20040126952 Gondhalekar et al. Jul 2004 A1
20040163669 Brueckner et al. Aug 2004 A1
20040180158 Lin et al. Sep 2004 A1
20040222088 Subramani et al. Nov 2004 A1
20040231798 Gondhalekar et al. Nov 2004 A1
20040251130 Liu et al. Dec 2004 A1
20040256226 Wickersham Dec 2004 A1
20040261946 Endoh et al. Dec 2004 A1
20050011749 Kachalov et al. Jan 2005 A1
20050028838 Brueckner Feb 2005 A1
20050048876 West et al. Mar 2005 A1
20050061857 Hunt et al. Mar 2005 A1
20050067469 Facey et al. Mar 2005 A1
20050089699 Lin et al. Apr 2005 A1
20050092604 Ivanov May 2005 A1
20050098427 Cho et al. May 2005 A1
20050147150 Wickersham et al. Jul 2005 A1
20050161322 Smathers Jul 2005 A1
20050172984 Schweitzer et al. Aug 2005 A1
20050178653 Fisher Aug 2005 A1
20050211548 Gung et al. Sep 2005 A1
20050238807 Lin Oct 2005 A1
20050271984 Brueckner et al. Dec 2005 A1
20050282358 Di Cioccio et al. Dec 2005 A1
20050284372 Murugesh et al. Dec 2005 A1
20060005767 Tsai et al. Jan 2006 A1
20060021870 Tsai et al. Feb 2006 A1
20060070876 Wu et al. Apr 2006 A1
20060090706 Miller et al. May 2006 A1
20060105182 Brueckner et al. May 2006 A1
20060108217 Krempel-Hesse et al. May 2006 A1
20060188742 West et al. Aug 2006 A1
20060251822 Gell et al. Nov 2006 A1
20060283703 Lee et al. Dec 2006 A1
20070059460 Abney et al. Mar 2007 A1
20070062452 Pancham et al. Mar 2007 A1
20070102286 Scheible et al. May 2007 A1
20070113783 Lee et al. May 2007 A1
20070125646 Young et al. Jun 2007 A1
20070170052 Ritchie et al. Jul 2007 A1
20070173059 Young et al. Jul 2007 A1
20070215463 Parkhe et al. Sep 2007 A1
20070274876 Chiu et al. Nov 2007 A1
20070283884 Tiller et al. Dec 2007 A1
20080038481 West et al. Feb 2008 A1
20080066785 Vesci et al. Mar 2008 A1
20080110760 Han et al. May 2008 A1
20080141942 Brown et al. Jun 2008 A1
20080178801 Pavloff et al. Jul 2008 A1
20080257263 Pavloff et al. Oct 2008 A1
20080295872 Riker et al. Dec 2008 A1
20090084317 Wu et al. Apr 2009 A1
20090120462 West et al. May 2009 A1
20090121604 Stahr et al. May 2009 A1
Foreign Referenced Citations (86)
Number Date Country
19719133 Nov 1998 DE
0239349 Sep 1987 EP
0439000 Jul 1991 EP
0601788 Jun 1994 EP
0 610 556 Aug 1994 EP
0635869 Jan 1995 EP
0791956 Aug 1997 EP
0818803 Jan 1998 EP
0838838 Apr 1998 EP
0845545 Jun 1998 EP
1049133 Nov 2000 EP
1094496 Apr 2001 EP
1158072 Nov 2001 EP
1258908 Nov 2002 EP
2562097 Oct 1985 FR
1424365 Feb 1976 GB
54-162969 Dec 1979 JP
54162696 Dec 1979 JP
11-59368 Dec 1987 JP
63235435 Sep 1988 JP
02-027748 Jan 1990 JP
02-101157 Apr 1990 JP
03-138354 Jun 1991 JP
06-232243 Aug 1994 JP
07-197272 Aug 1995 JP
09-017850 Jan 1997 JP
09-272965 Oct 1997 JP
10-045461 Feb 1998 JP
10-167859 Jun 1998 JP
63149396 Jun 1998 JP
10-251871 Sep 1998 JP
10-330971 Dec 1998 JP
11-137440 May 1999 JP
11-219939 Aug 1999 JP
11-220164 Aug 1999 JP
11-283972 Oct 1999 JP
2000-228398 Oct 1999 JP
2250990 Oct 1999 JP
11-345780 Dec 1999 JP
2000-072529 Mar 2000 JP
2000-191370 Jul 2000 JP
2002-69695 Mar 2002 JP
2002-187736 Jul 2002 JP
2005-134680 May 2005 JP
546680 Aug 2003 TW
WO-9523428 Aug 1995 WO
WO-9708734 Mar 1997 WO
WO-9742648 Nov 1997 WO
WO-9850599 Nov 1998 WO
WO-9852208 Nov 1998 WO
WO-9903131 Jan 1999 WO
WO-9913126 Mar 1999 WO
WO-9913545 Mar 1999 WO
WO-9914788 Mar 1999 WO
WO-9917336 Apr 1999 WO
WO-9928945 Jun 1999 WO
WO-9941426 Aug 1999 WO
WO-0005751 Feb 2000 WO
WO-0026939 May 2000 WO
WO-0184590 Nov 2001 WO
WO-0184624 Nov 2001 WO
WO-0215255 Feb 2002 WO
WO-0223587 Mar 2002 WO
WO 0293624 Nov 2002 WO
WO-03015137 Feb 2003 WO
WO-03057943 Jul 2003 WO
WO-03076683 Sep 2003 WO
WO-03083160 Oct 2003 WO
WO-03087427 Oct 2003 WO
WO-03090248 Oct 2003 WO
WO-2004010494 Jan 2004 WO
WO-2004012242 Feb 2004 WO
WO-2004015736 Feb 2004 WO
WO-2004074932 Sep 2004 WO
WO-2004094702 Nov 2004 WO
WO-2005021173 Mar 2005 WO
WO 2005071137 Aug 2005 WO
WO-2006053231 May 2006 WO
WO-2006073585 Jul 2006 WO
WO-2007-030824 Mar 2007 WO
WO 2007008999 Apr 2007 WO
WO 2008079722 Jul 2008 WO
WO-2008079722 Jul 2008 WO
WO-2008-133876 Nov 2008 WO
WO-2008-153785 Dec 2008 WO
WO-2008156794 Dec 2008 WO
Non-Patent Literature Citations (9)
Entry
http://dictionary.reference.com/browse/annealing copyright 2009.
Nakasuji, et al., “Low Voltage and High Speed Operating Electrostatic Wafer Chuck,” J. Vac. Sci. Technol. A, 10(6):3573-3578 (Nov./Dec. 1992).
Rosenberg, RW, “Increasing PVD Tool Uptime and Particle Control with Twin-Wire-Arc Spray Coatings”, Mar. 2001, p. 103-105, 108, 11, vol. 19, No. 3, Cannon Comm., Santa Monica, CA.
Tucker, Jr., Robert C., “Plasma and Detonation Gun Deposition Techniques and Coating Properties,” Union Carbide Corp., Coatings Service Dept., Indianapolis, IN, pp. 454-489.
Watanabe, et al., “Effect of Additives on the Electrostatic Force of Alumina Electrostatic Chucks,” J. of the Ceramic Soc. of Jpn., 100(1):1-6 (1992).
Watanabe, et al., “Electrostatic Force and Absorption Current of Alumina Electrostatic Chucks,” Jpn. J. Appl. Phy., 31(Pt1, No. 7):2145-2150 (1992).
Watanabe, et al., “Relationship Between Electrical Resistivity and Electrostatic Force of Alumina Electrostatic Chuck,” Jpn. J. Appl. Phy., 32(Pt1, No. 2):864-871 (1993).
Watanabe, et al., “Resistivity and Microstructure of Alumina Ceramics Added with TiO2 Fired in Reducing Atmosphere,” J. of the Ceramic Doc. of Jpn. Int. Ed., 101-1076-1083.
Wright et al., “Low Temperature Etch Chuck: Modeling and Experimental Results of Heat Transfer and Wafer Temperature,” J. Vac. Sci. Technol. A, 10(4):1065-1070(Jul./Aug. 1992).
Related Publications (1)
Number Date Country
20070014949 A1 Jan 2007 US